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PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome
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  1. Correspondence to:
 Isabella Ceccherini, Ph.D
 Laboratorio Genetica Molecolare, Istituto G Gaslini, L.go G Gaslini, 5, 16148 Genova, Italy; isa.cunige.it
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Citation

Matera I, Bachetti T, Puppo F, et al
PHOX2B mutations and polyalanine expansions correlate with the severity of the respiratory phenotype and associated symptoms in both congenital and late onset Central Hypoventilation syndrome

Publication history

  • Accepted November 17, 2003
  • Revised November 14, 2003
  • First published April 30, 2004.
Online issue publication 
April 30, 2004

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